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Original Articles

High phylogenetic diversity of Gallibacterium anatis is correlated with low biosecurity measures and management practices on poultry farms

, &
Pages 467-475 | Received 07 Jan 2020, Accepted 02 May 2020, Published online: 02 Jul 2020

References

  • Alispahic, M., Christensen, H., Hess, C., Razzazi-Fazeli, E., Bisgaard, M. & Hess, M. (2012). MALDI-TOF mass spectrometry confirms clonal lineages of Gallibacterium anatis between chicken flocks. Veterinary Microbiology, 160, 269–273. doi: 10.1016/j.vetmic.2012.05.032
  • Bisgaard, M. (1977). Incidence of pasteurella haemolytica in the respiratory tract of apparently healthy chickens and chickens with infectious bronchitis: characterisation of 213 strains. Avian Pathology, 6, 285–292. doi: 10.1080/03079457708418238
  • Bisgaard, M. (1993). Ecology and significance of pasteurellaceae in animals. Zentralblatt fur Bakteriologie, 279, 7–26. doi: 10.1016/S0934-8840(11)80487-1
  • Bojesen, A.M., Nielsen, O.L., Christensen, J.P. & Bisgaard, M. (2004). In vivo studies of Gallibacterium anatis infection in chickens. Avian Pathology, 33, 145–152. doi: 10.1080/03079450310001652059
  • Bojesen, A.M., Nielsen, S.S. & Bisgaard, M. (2003). Prevalence and transmission of haemolytic Gallibacterium species in chicken production systems with different biosecurity levels. Avian Pathology, 32, 503–510. doi: 10.1080/0307945031000154107
  • Bojesen, A.M., Vazquez, M.E., Robles, F., Gonzalez, C., Soriano, E.V., Olsen, J.E. & Christensen, H. (2007). Specific identification of Gallibacterium by a PCR using primers targeting the 16S rRNA and 23S rRNA genes. Veterinary Microbiology, 123, 262–268. doi: 10.1016/j.vetmic.2007.02.013
  • Christensen, H., Bisgaard, M., Bojesen, A.M., Mutters, R. & Olsen, J.E. (2003). Genetic relationship among avian isolates classified as Pasteurella haemolytica. “Actinobacillus salpingitidis” or Pasteurella anatis with proposal of Gallibacterium anatis gen. nov., comb. nov. and description of additional genomospecies within Gallibacterium gen. nov. International Journal of Systematic and Evolutionary Microbiology, 53, 275–287. doi: 10.1099/ijs.0.02330-0
  • Christensen, H., Kuhnert, P., Olsen, J.E. & Bisgaard, M. (2004). Comparative phylogenies of the housekeeping genes atpD, infB and rpoB and the 16S rRNA gene within the Pasteurellaceae. International Journal of Systematic and Evolutionary Microbiology, 54, 1601–1609. doi: 10.1099/ijs.0.03018-0
  • Dahllof, I., Baillie, H. & Kjelleberg, S. (2000). rpoB-based microbial community analysis avoids limitations inherent in 16S rRNA gene intraspecies heterogeneity. Applied and Environmental Microbiology, 66, 3376–3380. doi: 10.1128/AEM.66.8.3376-3380.2000
  • Davies, R. & Wales, A. (2019). Antimicrobial resistance on farms: a review including biosecurity and the potential role of disinfectants in resistance selection. Comprehensive Reviews in Food Science and Food Safety, 18, 753–774. doi: 10.1111/1541-4337.12438
  • De Zwaan, R., Van Ingen, J. & Van Soolingen, D. (2014). Utility of rpoB gene sequencing for identification of nontuberculous mycobacteria in the Netherlands. Journal of Clinical Microbiology, 52, 2544–2551. doi: 10.1128/JCM.00233-14
  • Elhamid, H., Lakany, H., Bekheet, A., Elbestawy, A. & Mataried, N. (2017). Pathogenicity of ten Gallibacterium anatis isolates in commercial broiler chickens. Alexandria Journal of Veterinary Sciences, 49, 42–49.
  • Hall, T.A. (1999). Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symposium Series, 40, 95–98.
  • Hasegawa, M., Kishino, H. & Yano, T.A. (1985). Dating of the human-ape splitting by a molecular clock of mitochondrial DNA. Journal of Molecular Evolution, 22, 160–174. doi: 10.1007/BF02101694
  • Jordan, F.T.W., Williams, N.J., Wattret, A. & Jones, T. (2005). Observations on salpingitis, peritonitis and salpingoperitonitis in a layer breeder flock. Veterinary Record, 157, 573–577. doi: 10.1136/vr.157.19.573
  • Khomtchouk, B.B., Hennessy, J.R. & Wahlestedt, C. (2017). Shinyheatmap: ultra fast low memory heatmap web interface for big data genomics. PLoS One, 12, 1–9. doi: 10.1371/journal.pone.0176334
  • Kim, B.J., Lee, S.H., Lyu, M.A., Kim, S.J., Bai, G.H., Kim, S.J., Chae, G.T., Kim, E.C., Cha, C.Y. & Kook, Y.H. (1999). Identification of mycobacterial species by comparative sequence analysis of the RNA polymerase gene (rpoB). Journal of Clinical Microbiology, 37, 1714–1720. doi: 10.1128/JCM.37.6.1714-1720.1999
  • Korczak, B., Christensen, H., Emler, S., Frey, J. & Kuhnert, P. (2004). Phylogeny of the family Pasteurellaceae based on rpoB sequences. International Journal of Systematic and Evolutionary Microbiology, 54, 1393–1399. doi: 10.1099/ijs.0.03043-0
  • Kristensen, B.M., Frees, D. & Bojesen, A.M. (2011). Expression and secretion of the RTX-toxin GtxA among members of the genus Gallibacterium. Veterinary Microbiology, 153, 116–123. doi: 10.1016/j.vetmic.2011.05.019
  • Kumar, S., Stecher, G., Li, M., Knyaz, C. & Tamura, K. (2018). MEGA x: molecular evolutionary genetics analysis across computing platforms. Molecular Biology and Evolution, 35, 1547–1549. doi: 10.1093/molbev/msy096
  • Lawal, J.R., Ndahi, J.J., Bello, A.M., Wakil, Y., Dauda, J. & Ibrahim, U.I. (2017). Prevalence, isolation and antimicrobial susceptibility of Gallibacterium anatis from local breed of female Muscovy ducks (Cairina moschata) in Maiduguri, Northeastern Nigeria. Direct Research Journal of Veterinary Medicine and Animal Science, 2, 27–37.
  • Mollet, C., Drancourt, M. & Raoult, D. (1997). rpoB sequence analysis as a novel basis for bacterial identification. Molecular Microbiology, 26, 1005–1011. doi: 10.1046/j.1365-2958.1997.6382009.x
  • Neubauer, C., De Souza-Pilz, M., Bojesen, A.M., Bisgaard, M. & Hess, M. (2009). Tissue distribution of haemolytic Gallibacterium anatis isolates in laying birds with reproductive disorders. Avian Pathology, 38, 1–7. doi: 10.1080/03079450802577848
  • Paudel, S., Alispahic, M., Liebhart, D., Hess, M. & Hess, C. (2013). Assessing pathogenicity of Gallibacterium anatis in a natural infection model: the respiratory and reproductive tracts of chickens are targets for bacterial colonization. Avian Pathology, 42, 527–535. doi: 10.1080/03079457.2013.843160
  • Paudel, S., Hess, M. & Hess, C. (2017). Coinfection of Avibacterium paragallinarum and Gallibacterium anatis in specific-pathogen-free chickens complicates clinical signs of infectious Coryza, which can be prevented by vaccination. Avian Diseases, 61, 55–63. doi: 10.1637/11481-081016-Reg
  • Paudel, S., Liebhart, D., Aurich, C., Hess, M. & Hess, C. (2014). Pathogenesis of Gallibacterium anatis in a natural infection model fulfils Koch’s postulates: 2. Epididymitis and decreased semen quality are the predominant effects in specific pathogen free cockerels. Avian Pathology, 43, 529–534. doi: 10.1080/03079457.2014.967176
  • Paudel, S., Liebhart, D., Hess, M. & Hess, C. (2014). Pathogenesis of Gallibacterium anatis in a natural infection model fulfils Koch’s postulates: 1. Folliculitis and drop in egg production are the predominant effects in specific pathogen free layers. Avian Pathology, 43, 443–449. doi: 10.1080/03079457.2014.955782
  • Persson, G. & Bojesen, A.M. (2015). Bacterial determinants of importance in the virulence of Gallibacterium anatis in poultry. Veterinary Research, 46, 1–11. doi: 10.1186/s13567-015-0206-z
  • Renesto, P., Gouvernet, J., Drancourt, M., Roux, V. & Raoult, D. (2001). Use of rpoB gene analysis for detection and identification of Bartonella species. Journal of Clinical Microbiology, 39, 430–437. doi: 10.1128/JCM.39.2.430-437.2001
  • Renesto, P., Lorvellec-Guillon, K., Drancourt, M. & Raoult, D. (2000). rpoB gene analysis as a novel strategy for identification of spirochetes from the genera borrelia, treponema, and leptospira. Journal of Clinical Microbiology, 38, 2200–2203. doi: 10.1128/JCM.38.6.2200-2203.2000
  • Shaw, D.P., Cook, D.B., Maheswaran, S.K., Lindeman, C.J. & Halvorson, D.A. (1990). Pasteurella haemolytica as a co-pathogen in pullets and laying hens. Avian Diseases, 34, 1005–1008. doi: 10.2307/1591397
  • Varan Singh, S. & Singh, B.R. (2015). Gallibacterium anatis: an emerging pathogen of poultry birds and domiciled birds. Journal of Veterinary Science & Technology, 7, 324–330. doi: 10.4172/2157-7579.1000324
  • Wang, C., Robles, F., Ramirez, S., Riber, A.B. & Bojesen, A.M. (2016). Culture-independent identification and quantification of Gallibacterium anatis (G. anatis) by real-time quantitative PCR. Avian Pathology, 45, 538–544. doi: 10.1080/03079457.2016.1184743

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